ea0028s3.4 | Testosterone in men: how long can you go? | SFEBES2012
Raivio Taneli
Congenital hypogonadotropic hypogonadism (HH) is characterized by deficient secretion and/or action of GnRH. The combination of hyposmia/anosmia and HH is termed Kallmann syndrome (minimal incidence estimate for men 1:30 000 and 1:125 000 in women, Laitinen et al. OJRD 2011), and, when the sense of smell is intact, normosmic HH (nHH). Even 10% of CHH patients may undergo reversal of hypogonadotropism after the age of 20 yrs (Raivio T et al. NEJM 2007), and the mo...